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Development of lithium ion kinetic, bottleneck for microscale particle of disordered rock-salt(DRX) cathode material by Cr doping

Author(s)
Chung, Yubin
Advisor
Jung, Sung-Kyun
Issued Date
2024-08
URI
https://scholarworks.unist.ac.kr/handle/201301/84153 http://unist.dcollection.net/common/orgView/200000814263
Abstract
With the increasing demand for electric vehicles (EVs), interest in affordable and high-energy-density batteries has been growing. To reduce battery costs while enhancing energy density, research on cathode materials is crucial. Among these, disordered rock-salt (DRX) has been proposed as a next-generation cathode material. It utilizes Mn as a redox center in a Li-rich environment and offers the application of various transition metals, providing advantages in both cost and energy density. However, the intrinsic Li+ diffusivity in DRX materials is typically low (DLi: 10-16–10-15 cm2/s) unless 0-TM percolation is organically established, as the Li-ion pathway is randomly formed. Therefore, conventional DRX materials have been utilized in nanometer sizes to minimize the Li-ion pathway. Attaining high capacity and rate capability with micrometer-sized Mn-DRX particles, which necessitate long-range Li diffusion, has not yet been accomplished. Instead, the synthesized particles typically undergo a pulverization process using a planetary ball mill or shaker mill, often combined with conductive carbon black, to create an Mn-DRX-carbon black composite. Following this process, the Mn-DRX particles are reduced to nano size (e.g., d < 200 nm), typically resulting in the broadening of XRD peaks. The DRX-carbon black composite powder is then mixed with binders to synthesize the Mn-DRX cathode film. So far, the most frequently used weight ratio between the Mn-DRX, carbon black, and binder in the cathode film has been 70:20:10, with a minimum carbon loading of 10 wt %, which is unacceptably high for practical cathodes. So, even though DRX has a high energy density per weight, it inevitably has a low energy density per volume. Such energy density per volume can be improved through sizing up; however, DRX requires higher Li-ion conductivity compared to the existing nanoscale materials to achieve this upscaling. Therefore, in this study, I introduce DRX material in a more practical environment by growing particle size (micro-scale) following the previous study of improving Li+ kinetic characteristics through Cr doping. Li1.2Mn0.4Ti0.4O2 (LMTO) and the Cr-doped material Li1.2Mn0.2Ti0.4Cr0.2O2 (LMTCO) are compared to evaluate the Li+ kinetic differences between the existing DRX material (LMTO) and the Cr-doped DRX material (LMTCO) in terms of size. As a result, the increase in capacity ratio due to the effect of Cr tetrahedral migration is minimal in the original nano-sized DRX materials but increased more significantly in the larger sub-micro-sized DRX materials. It demonstrated superior energy density per volume compared to the existing nanoscale materials, and this improved effect was more pronounced in the Cr-doped materials. This finding is supported by various analyses, suggesting that this strategy and design could allow for an approach to slightly larger sizes in DRX.
Publisher
Ulsan National Institute of Science and Technology
Degree
Master
Major
School of Energy and Chemical Engineering (Energy Engineering(Battery Science and Technology))

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